AR122911A1 - Proceso e intermediarios para la preparación de piroxasulfona, fenoxasulfona y varios análogos sulfona de 5,5-dimetil-4h-1,2-oxazol - Google Patents

Proceso e intermediarios para la preparación de piroxasulfona, fenoxasulfona y varios análogos sulfona de 5,5-dimetil-4h-1,2-oxazol

Info

Publication number
AR122911A1
AR122911A1 ARP210101918A ARP210101918A AR122911A1 AR 122911 A1 AR122911 A1 AR 122911A1 AR P210101918 A ARP210101918 A AR P210101918A AR P210101918 A ARP210101918 A AR P210101918A AR 122911 A1 AR122911 A1 AR 122911A1
Authority
AR
Argentina
Prior art keywords
formula
protecting group
compounds
isoxazoline
preparation
Prior art date
Application number
ARP210101918A
Other languages
English (en)
Inventor
Yaniv Barda
Nitsan Papo
Carl Recsei
Original Assignee
Adama Agan Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Adama Agan Ltd filed Critical Adama Agan Ltd
Publication of AR122911A1 publication Critical patent/AR122911A1/es

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/04—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
    • C07C41/22—Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of halogens; by substitution of halogen atoms by other halogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00—Ethers; Compounds having groups, groups or groups
    • C07C43/02—Ethers
    • C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
    • C07C43/225—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/18—One oxygen or sulfur atom
    • C07D231/20—One oxygen atom attached in position 3 or 5
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La invención se refiere a un proceso para la preparación de precursores inmediatos para la preparación de piroxasulfona y fenoxasulfona de fórmula (1). El proceso comprende una reacción de bromación de una posición bencílica sin irradiación de luz (etapa a), seguido de una reacción de tionación, que sustituye al átomo de bromo (etapa b) y después eliminar el grupo protector, y el tiol o tiolato revelado reacciona con una isoxazolina sustituida que lleva un grupo saliente en la posición 3 (etapa c). Esquemas 1 y 2, en donde Y = grupo protector. En otra variante de la invención los precursores inmediatos de piroxasulfona o fenoxasulfona se sintetizan a partir de bromuro de arilmetilo formando en primer lugar un enlace carbono-azufre en la posición 3 de una 2-isoxazolina a través del desplazamiento de un grupo saliente en la posición 3 (particularmente restos derivados ácidos tales como grupos fosforilo, sulfanilo, halo, ciano o carboxilo) mediante un reactivo tionante apropiado. Los aductos resultantes, que es una 3-tio-2-isoxazolina S-protegida, se pueden tratar con base para eliminar el grupo protector, para revelar un tiol o tiolato que posteriormente puede reaccionar con el bromuro de arilmetilo para formar el precursor inmediato piroxasulfona o fenoxasulfona. Esquema 3, Ar = arilo, Y = grupo protector y X = grupo saliente. Reivindicación 1: Un proceso para preparar compuestos de las fórmulas (1) ó (1’) que comprende las siguientes etapas: a) bromación de un material de partida seleccionado de los siguientes compuestos: de fórmula (4) ó (4’) para obtener los siguientes compuestos: de fórmula (3) ó (3’) respectivamente; b) tionación del compuesto resultante de la etapa a con un agente tionante para obtener los siguientes compuestos: de fórmula (2) ó (2’) respectivamente en donde Y es un grupo protector; c) sustitución del tiol o tiolato resultante creado a partir de los compuestos de fórmulas (2) ó (2’) de la etapa b por un resto 2-isoxazolina para producir el compuesto de fórmula (1). Reivindicación 7: Un proceso para preparar un compuesto de fórmulas (3) ó (3’) que comprende compuestos de bromación de fórmulas (4) ó (4’), respectivamente, con un reactivo de bromación en ausencia de irradiación de luz.
ARP210101918A 2020-07-10 2021-07-08 Proceso e intermediarios para la preparación de piroxasulfona, fenoxasulfona y varios análogos sulfona de 5,5-dimetil-4h-1,2-oxazol AR122911A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP20185255.5A EP3936503A1 (en) 2020-07-10 2020-07-10 Process and intermediates for the preparation of pyroxasulfone, fenoxasulfone and various sulfone analogs of 5,5-dimethyl-4h-1,2-oxazole

Publications (1)

Publication Number Publication Date
AR122911A1 true AR122911A1 (es) 2022-10-12

Family

ID=71575178

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP210101918A AR122911A1 (es) 2020-07-10 2021-07-08 Proceso e intermediarios para la preparación de piroxasulfona, fenoxasulfona y varios análogos sulfona de 5,5-dimetil-4h-1,2-oxazol

Country Status (10)

Country Link
US (1) US20230234947A1 (es)
EP (4) EP4177244A3 (es)
JP (1) JP2023533571A (es)
KR (1) KR20230038520A (es)
CN (1) CN115836067A (es)
AR (1) AR122911A1 (es)
BR (1) BR112023000266A2 (es)
IL (1) IL299509A (es)
UY (1) UY39319A (es)
WO (1) WO2022009044A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114716379A (zh) * 2022-05-13 2022-07-08 绍兴贝斯美化工股份有限公司 一种砜吡草唑中间体的制备方法
CN117229273B (zh) * 2023-11-13 2024-02-02 江苏七洲绿色化工股份有限公司 一种砜吡草唑及其中间体的制备方法

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4465133B2 (ja) 2001-02-08 2010-05-19 クミアイ化学工業株式会社 イソオキサゾリン誘導体及びこれを有効成分とする除草剤
JP2004002324A (ja) * 2002-03-22 2004-01-08 Kumiai Chem Ind Co Ltd 除草剤組成物
CA2494130C (en) 2002-08-01 2011-08-23 Ihara Chemical Industry Co., Ltd. Pyrazole derivatives and process for the production thereof
JP4621939B2 (ja) 2004-03-31 2011-02-02 イハラケミカル工業株式会社 ５−ヒドロキシ−４−チオメチルピラゾール化合物の製造方法
CA2577495C (en) * 2004-09-03 2013-08-06 Syngenta Limited Isoxazoline derivatives and their use as herbicides
JP2008001597A (ja) 2004-10-06 2008-01-10 Ihara Chem Ind Co Ltd ３−ブロモ−５，５−ジメチル−４，５−ジヒドロイソオキサゾールの製造方法
NZ554870A (en) 2004-12-20 2009-09-25 Ihara Chemical Ind Co Process for production of (4,5-dihydroisoxazol-3-Yl)thio- carboxamidine salts
DE102005006306A1 (de) 2005-02-11 2006-08-17 Rehau Ag + Co Bausatz für die Montage eines Fahrzeugverkleidungselements
GB0526044D0 (en) 2005-12-21 2006-02-01 Syngenta Ltd Novel herbicides
DE102005063066A1 (de) 2005-12-29 2007-07-05 Bayer Cropscience Gmbh 2-[Pyrazolyl-methan-sulfonyl])-pyridin-N-oxid-Derivate und 2-[Pyrazlyl-methan-sulfinyl])-pyridin-N-oxid-Derivate, Verfahren zu deren Herstellung und Verwendung als Herbizide und Pflanzenwachstumsregulatoren
GB0603891D0 (en) * 2006-02-27 2006-04-05 Syngenta Ltd Novel herbicides
AU2007332476A1 (en) * 2006-12-14 2008-06-19 Taisho Pharmaceutical Co., Ltd. 1-phenyl 1-thio-D-glucitol derivative
CL2008000376A1 (es) * 2007-02-09 2008-08-18 Du Pont Compuestos derivados de n-oxidos de piridina; composicion herbicida; y metodo para controlar el crecimiento de vegetacion indeseada.
WO2008114493A1 (ja) * 2007-03-16 2008-09-25 Kumiai Chemical Industry Co., Ltd. 除草剤組成物
EP2065374A1 (de) 2007-11-30 2009-06-03 Bayer CropScience AG 2-(Benzyl- und 1H-pyrazol-4-ylmethyl)sulfinyl-Thiazol-Derivate als Herbizide und Pflanzenwachstumsregulatoren
EP2112149A1 (de) 2008-04-22 2009-10-28 Bayer CropScience Aktiengesellschaft 2-[(1h-Pyrazol-4-ylmethyl)-sulfonyl]-Oxazol-Derivate, 2-[(1H-Pyrazol-4-ylmethyl)-sulfanyl]-Oxazol-Derivate und chirale 2-[(1H-Pyrazol-4-ylmethyl)-sulfinyl]-Oxazol-Derivate, Verfahren zu deren Herstellung sowie deren Verwendung als Herbizide und Pflanzenwachstumsregulatoren
AU2010261874B2 (en) 2009-06-19 2015-05-14 Basf Se Herbicidal benzoxazinones
UY32838A (es) 2009-08-14 2011-01-31 Basf Se "composición activa herbicida que comprende benzoxazinonas
KR20120112487A (ko) 2009-11-26 2012-10-11 바스프 에스이 ５,５-이치환된 ２-이속사졸린의 제조 방법
MX2012005884A (es) * 2009-11-26 2012-06-19 Basf Se Metodo para producir sales de 4,5-dihidroisoxazol-3-tiocarboxamidi na 5,5-disustituida.
EP3194393B1 (en) 2014-09-19 2020-03-11 ISAGRO S.p.A. 1,3,4-thiadiazoles having a herbicidal activity, their agronomical compositions and relative use
CN109836391B (zh) * 2017-11-24 2019-12-27 东莞市东阳光农药研发有限公司 异噁唑啉衍生物及其在农业中的应用

Also Published As

Publication number Publication date
IL299509A (en) 2023-02-01
UY39319A (es) 2021-12-31
EP4177245A1 (en) 2023-05-10
EP3936503A1 (en) 2022-01-12
EP4177252A3 (en) 2023-08-09
KR20230038520A (ko) 2023-03-20
EP4177244A3 (en) 2023-08-09
WO2022009044A1 (en) 2022-01-13
BR112023000266A2 (pt) 2023-01-31
EP4177252A2 (en) 2023-05-10
US20230234947A1 (en) 2023-07-27
CN115836067A (zh) 2023-03-21
EP4177244A2 (en) 2023-05-10
JP2023533571A (ja) 2023-08-03

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